Our
client, a world leader in biotechnology and life sciences, is looking for
a
“QC Lead Investigator/Event Owner (Laboratory Equipment)” based out
of Philadelphia, PA.

Job Duration: Long Term Contract (Possibility Of
Extension)

Pay Rate : $46/hr on W2

Company Benefits:
Medical, Dental, Vision, Paid Sick leave, 401K

The Quality Control (QC) team is seeking a
Laboratory
Equipment Investigation Lead
responsible for managing investigations,
deviations, change controls, and CAPAs related to QC laboratory equipment and
systems. The role ensures compliance with
cGMP regulations and internal
quality procedures
, while supporting QC operations and regulatory
readiness.

Key Responsibilities:

·
Conduct and manage
QC
laboratory equipment investigations, deviations, and quality incidents
.

·
Identify root causes
and implement
Corrective and Preventive Actions (CAPAs)
.

·
Author and manage
change
controls
for laboratory equipment, systems, and software.

·
Serve as
system
administrator for QC laboratory systems
(user access, templates, method
controls).

·
Collaborate with
QC,
Lab Systems Engineering, QA, IT, and cross-functional teams
.

·
Perform
risk and
impact assessments
for QC operations.

·
Support
regulatory
inspections and audits
.

·
Maintain
cGMP
documentation
and update SOPs and supporting documents as required.

Qualifications:

·
Bachelor’s degree in
Science,
Engineering, Quality, or related field
(or equivalent experience).

·
Experience in
QC,
QA, or regulated biotech/pharmaceutical environments
.

·
Knowledge of
cGMP,
FDA regulations, and quality systems
.

·
Familiarity with
laboratory systems such as
Empower, LabX, SoftMax, qPCR, or similar
preferred.

·
Experience with
Veeva
Vault QMS
and root cause analysis methods (5 Whys, Fishbone, FMEA)
preferred.

·
Strong analytical,
documentation, and cross-functional collaboration skills.

If interested, please send us your updated resume at

hr@dawarconsulting.com
/
akansha@dawarconsulting.com